Canonical Allele Identifier: CA994818

Gene: GSTM3 GSTM5

Linked Data

• dbSNP Id: rs771594653
• ExAC: 1:110279701 C / CGG
• gnomAD v2: 1-110279701-C-CGG
• MyVariant Identifiers: chr1:g.110279701_110279702insGG (hg19) ; chr1:g.109737079_109737080insGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737079_109737080insGG , CM000663.2:g.109737079_109737080insGG	GRCh38
NC_000001.10:g.110279701_110279702insGG , CM000663.1:g.110279701_110279702insGG	GRCh37
NC_000001.9:g.110081224_110081225insGG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361066.7:c.669_670insCC (GSTM3) MANE Select	ENSP00000354357.2:p.Val224ProfsTer?
ENST00000256594.7:c.669_670insCC (GSTM3)	ENSP00000256594.3:p.Val224ProfsTer?
ENST00000361066.6:c.669_670insCC (GSTM3)	ENSP00000354357.2:p.Val224ProfsTer?
ENST00000429410.2:n.82+24731_82+24732insGG (GSTM5)
ENST00000476321.5:n.637_638insCC (GSTM3)
ENST00000486823.5:n.633_634insCC (GSTM3)
ENST00000488824.1:n.1014_1015insCC (GSTM3)
NM_000849.4:c.669_670insCC (GSTM3)	NP_000840.2:p.Val224ProfsTer?
NR_024537.1:n.903_904insCC (GSTM3)
XM_011541296.1:c.888_889insCC (GSTM3)	XP_011539598.1:p.Val297ProfsTer?
NM_000849.5:c.669_670insCC (GSTM3) MANE Select	NP_000840.2:p.Val224ProfsTer?
NR_024537.2:n.903_904insCC (GSTM3)